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1152552-07-2

6-Chloro-3-cyclopropyl-[1,2,4]triazolo[4,3-b]pyridazine synthesis

2synthesis methods
-

Yield:1152552-07-2 170 mg

Reaction Conditions:

with acetic acid in toluene at 120; for 0.5 h;Microwave irradiation;

Steps:

8 Synthesis of A-9:

A mixture of A-2 (200.00 mg, 1.38 mmol) and cyclopropanecarbonyl chloride (150.54 _^, 1.66 mmol) in toluene (10 mL) was stirred at 100 C for 12 hour. This mixture was concentrated and AcOH (10 mL) was added to the residue. The mixture was stirred at 120 C for 0.5 hour in a microwave reactor, then the mixture was concentrated, diluted with H20 (10 mL), basified with solid NaHC03 to pH ~ 9, extracted with EtOAc (30 mL x 2), and the combined organic phase was washed with brine (10 mL), dried over Na2S04, filtered and concentrated to give crude A-9 (170.00 mg). LCMS Rt = 0.64 min using Method B, MS ESI calcd. for C8H8C1N4 [M+H]+194.9, found 195.0.

References:

WO2018/98499,2018,A1 Location in patent:Page/Page column 125